| Literature DB >> 31134883 |
Ravindra Kumar Garg1, Neeraj Kumar1, Imran Rizvi1, Amita Jain2, Ravi Shekhar Jaipuriar1, Praveen Kumar Sharma1, Hardeep Singh Malhotra1, Danish Nasar Khan2, Ravi Uniyal1.
Abstract
Subacute sclerosing panencephalitis (SSPE) is still a common disease in India which is characterized by a progressive mental decline, myoclonus, periodic encephalographic abnormalities, and raised anti-measles antibody titter in the cerebrospinal fluid. Acute fulminant SSPE is characterized by a rapid course of disease culminating in death, within 6 months. We report of a 10-year-old boy, who came with a 14-day history of continuous involuntary jerky movements of the left half of the body, including the head. There was a highly increased anti-measles IgG antibody titer, both in the cerebrospinal fluid and serum. We conclude that acute rapidly progressive SSPE can present as acute encephalitis syndrome.Entities:
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Year: 2019 PMID: 31134883 PMCID: PMC6609179 DOI: 10.4269/ajtmh.19-0215
Source DB: PubMed Journal: Am J Trop Med Hyg ISSN: 0002-9637 Impact factor: 2.345